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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631972copy number variation1nstd224human GRCh37 chr7: 57,188,377-57,531,189 , GRCh38.p12 chr7: 57,120,670-57,471,483 GUSBP10, MTND5P6, 30 more genes
    nsv6600936copy number variation1nstd223human GRCh38 chr7: 57,137,444-57,138,386 , GRCh37.p13 chr7: 57,205,151-57,206,093 ZNF479
    nsv6558053inversion1nstd223human GRCh38 chr7: 57,139,945-57,141,372 , GRCh37.p13 chr7: 57,207,652-57,209,079 ZNF479
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv5564983copy number variation1nstd207human GRCh38 chr7: 57,116,581-57,118,562 , GRCh37.p13 chr7|NW_003571039.1: 348,679-350,660 , GRCh37.p13 chr7: 57,184,288-57,186,269 ZNF479
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5482153copy number variation1nstd206human GRCh38 chr7: 56,993,800-57,540,242 , GRCh37.p13 chr7: 57,190,580-57,599,948 , MTCYBP29, 39 more genes
    nsv5239881copy number variation1nstd204human GRCh38.p13 chr7: 57,124,401-57,127,700 , GRCh37.p13 chr7: 57,192,108-57,195,407 ZNF479
    nsv5228777copy number variation1nstd204human GRCh38.p13 chr7: 57,124,347-57,126,545 , GRCh37.p13 chr7: 57,192,054-57,194,252 ZNF479
    nsv5227661copy number variation1nstd204human GRCh38.p13 chr7: 57,124,709-57,126,779 , GRCh37.p13 chr7: 57,192,416-57,194,486 ZNF479
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956891copy number variation1nstd200human GRCh38 chr7: 57,056,195-63,228,539 , GRCh37.p13 chr7: 57,190,578-62,688,917 , SEPTIN7P15, 50 more genes
    nsv4765725inversion1nstd199human GRCh37 chr7: 57,119,077-62,979,736 , GRCh38.p12 chr7: 57,051,370-63,519,358 , ZNF479, 70 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4684255copy number variation1nstd102humanUncertain significance GRCh37 chr7: 57,127,051-57,528,311 , GRCh38.p12 chr7: 57,059,344-57,468,605 MTATP6P8, NMTRQ-TTG13-1, 33 more genes
    nsv4679115copy number variation1nstd189human GRCh37.p13 chr7: 56,818,765-57,582,095 , GRCh38.p12 chr7: 56,751,072-57,522,389 , ZNF479, 53 more genes
    nsv4612767copy number variation1nstd183human GRCh37 chr7: 56,701,214-58,007,147 , GRCh38.p12 chr7: 56,633,521-57,947,441 , LOC105375289, 66 more genes
    nsv4608784copy number variation1nstd183human GRCh37 chr7: 56,697,186-58,019,983 , GRCh38.p12 chr7: 56,629,493-57,960,277 , VN1R26P, 67 more genes
    nsv4604087copy number variation1nstd183human GRCh37 chr7: 57,130,914-57,863,811 , GRCh38.p12 chr7: 57,063,207-57,804,105 , SAPCD2P2, 40 more genes
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